Brennan J C, MacLaren D A
SUPA, School of Physics & Astronomy, University of Glasgow, Glasgow, UK.
J Microsc. 2025 Jan;297(1):35-42. doi: 10.1111/jmi.13348. Epub 2024 Aug 8.
Electron energy loss spectra collected from fresh and corroded silver nanoparticles are compared with those from a number of reference materials, focusing on the M edge. Chemical shifts and changes in the energy loss near edge structure (ELNES) are described and found to be sufficient to distinguish metallic silver from chemically oxidised silver. The measurements, in conjunction with electron energy loss spectrum imaging, are used to assess the mechanisms for atmospheric corrosion of silver nanoparticles. We unambiguously assign the corrosion product under atmospheric conditions to be silver sulphide, but show the reaction process to be distinctly inhomogeneous, producing a variety of types of corroded particles. LAY DESCRIPTION: >Here, we use analytical electron microscopy to track the corrosion of silver nanoparticles and present chemical maps of the corrosion products. We show clear spectroscopic differences between metallic and corroded silver using the M electron energy loss spectral feature, which is not commonly studied. Our study shows that corrosion is due to interactions with sulphur in the atmosphere; and the corrosion is not uniform, but appears to develop from specific points on the surface of the nanoparticles.
将从新鲜的和腐蚀后的银纳米颗粒收集的电子能量损失谱与从多种参考材料收集的谱进行比较,重点关注M边。描述了化学位移和近边能量损失结构(ELNES)的变化,发现这些足以区分金属银和化学氧化银。这些测量结合电子能量损失谱成像,用于评估银纳米颗粒的大气腐蚀机制。我们明确确定大气条件下的腐蚀产物为硫化银,但表明反应过程明显不均匀,产生了多种类型的腐蚀颗粒。 层面描述:>在这里,我们使用分析电子显微镜追踪银纳米颗粒的腐蚀情况,并展示腐蚀产物的化学图谱。我们利用不常研究的M电子能量损失谱特征,展示了金属银和腐蚀银之间明显的光谱差异。我们的研究表明,腐蚀是由于与大气中的硫相互作用所致;而且腐蚀并不均匀,似乎是从纳米颗粒表面的特定点开始发展的。